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乳果糖联合液状石蜡与聚乙二醇治疗功能性便秘的疗效和安全性比较:一项随机临床试验。

Comparative efficacy and safety of lactulose plus paraffin vs polyethylene glycol in functional constipation: a randomised clinical study.

机构信息

University of Nice Sophia Antipolis, Nice, France.

Unit of Medical Oncology, Department of Gastroenterology, CHU Nice, Nice, France.

出版信息

United European Gastroenterol J. 2020 Oct;8(8):923-932. doi: 10.1177/2050640620937913. Epub 2020 Jun 28.

Abstract

BACKGROUND

Few head-to-head comparisons of the different classes of laxatives have been conducted.

OBJECTIVE

The objective of this work is to compare the efficacy of lactulose plus paraffin vs polyethylene glycol in the treatment of functional constipation (non-inferiority study).

METHODS

This randomised, parallel-group, multicentre phase 4 study recruited patients with functional constipation diagnosed according to Rome III criteria. Patients received lactulose plus paraffin or polyethylene glycol for 28 days. The primary end point was the change from baseline in the Patient Assessment of Constipation-Symptoms (PAC-SYM) score.

RESULTS

A total of 363 patients were randomised to lactulose plus paraffin ( = 179) or polyethylene glycol ( = 184). On day 28, the mean PAC-SYM score decreased significantly vs baseline with both treatments ( < 0.001). The lower boundary of the 95% CI exceeded the pre-specified limit of -0.25, therefore establishing non-inferiority of lactulose plus paraffin vs polyethylene glycol. At least one adverse event occurred in 20 patients (11.2%) in the lactulose plus paraffin group and in 26 patients (14.2%) in the polyethylene glycol group, most of which were of mild or moderate severity and unrelated to study drugs.

CONCLUSION

Lactulose plus paraffin may be used interchangeably with polyethylene glycol for the pharmacological treatment of functional constipation. EudraCT number 2015-003021-34.

摘要

背景

很少有针对不同类泻药的头对头比较。

目的

本研究旨在比较乳果糖加石蜡与聚乙二醇在功能性便秘(非劣效性研究)治疗中的疗效。

方法

这是一项随机、平行分组、多中心的 4 期研究,招募了根据罗马 III 标准诊断为功能性便秘的患者。患者接受乳果糖加石蜡或聚乙二醇治疗 28 天。主要终点是患者便秘症状自评量表(PAC-SYM)评分从基线的变化。

结果

共有 363 名患者被随机分配至乳果糖加石蜡组(n=179)或聚乙二醇组(n=184)。第 28 天,与基线相比,两组的 PAC-SYM 评分均显著下降(均<0.001)。95%CI 的下限超过了预设的-0.25 界限,因此确立了乳果糖加石蜡与聚乙二醇的非劣效性。乳果糖加石蜡组有 20 名患者(11.2%)和聚乙二醇组有 26 名患者(14.2%)至少发生了 1 次不良事件,大多数为轻中度,与研究药物无关。

结论

乳果糖加石蜡可与聚乙二醇交替用于功能性便秘的药物治疗。EudraCT 编号 2015-003021-34。

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